Component

SELENOF

Independent protein record for Selenoprotein F.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. SELENOF associates with human UGGT1 in binding and photo-crosslinking experiments involving ER glycoprotein quality-control proteins.

    SELENOF → UGGT1 source_derived_draftliterature_reviewed:direct_experimental
    Experimental context and source evidence
    experimental_model
    Recombinant SELENOF and truncated human UGGT1 binding/crosslinking assays.
    limitations
    Binding is directly measured; exact physiological glycoprotein substrates and obligatory disulfide-repair steps are not established by this result.
    organism
    Human protein constructs

    Selenium: literature corrections and mechanism additions · lines 1053–1062

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · Recombinant SELENOF and truncated human UGGT1 binding/crosslinking assays. · secondary_verified · secondary_verified

    ## selenof-binds-uggt1 SELENOF partners with a protein-folding inspection enzyme. SELENOF associates with human UGGT1 in binding and photo-crosslinking experiments involving ER glycoprotein quality-control proteins. Experimental model: Recombinant SELENOF and truncated human UGGT1 binding/crosslinking assays. Organism: Human protein constructs Limitations: Binding is directly measured; exact physiological glycoprotein substrates and obligatory disulfide-repair steps are not established by this result. Primary reference: [Analysis of Selenoprotein F Binding to UDP-Glucose:Glycoprotein Glucosyltransferase by a Photoreactive Crosslinker](https://pubmed.ncbi.nlm.nih.gov/36219527/)
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards